机译:全球罕见拷贝数变异对自闭症谱系障碍的功能影响
The Centre for Applied Genomics and Program in Genetics and Genomic Biology, The Hospital for Sick Children, Toronto, Ontario M5G 1L7, Canada;
rnWellcome Trust Centre for Human Genetics, University of Oxford, Oxford 0X3 7BN, UK;
rnDepartment of Psychiatry, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania 15213, USA;
rnAutism Genetics Group, Department of Psychiatry, School of Medicine, Trinity College, Dublin 8, Ireland;
rnBanting and Best Department of Medical Research, Terrence Donnelly Centre for Cellular and Biomolecular Research, University of Toronto, Toronto, Ontario M5S 3E1, Canada;
et al;
机译:稀有基因组拷贝数变异的预测对自闭症谱系统疾病兄弟姐妹的影响
机译:罕见拷贝数变异的鉴定揭示了PJA2,APC,SYNPO和TAC1作为自闭症谱系疾病中的新型候选基因
机译:自闭症谱系障碍个体中稀有拷贝数变异的发现资源
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机译:稀有基因组拷贝数变异对自闭症谱系疾病婴幼儿兄弟姐妹的预测影响
机译:在自闭症全球罕见的拷贝数变异功能影响
机译:自闭症谱系障碍中全球罕见拷贝数变异的功能影响。